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myelin associated glycoprotein  (Bioss)


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    Bioss myelin associated glycoprotein
    Figure 4. miR‑210 has an effect on the protein levels of GAP‑43, MAG and MBP. (A and B) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of GAP‑43 were detected by western blot analysis. Relative protein levels were calculated using β‑actin as an internal reference. (C and D) The protein levels of MBP were detected by western blot after transfection with miR‑210 mimics or miR‑210 inhibitor. β‑actin was used as an internal reference. (E and F) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of MAG were detected by western blot using β‑actin as an internal reference. All experiments were repeated three times and values are expressed as the mean ± standard deviation. **P<0.01, ***P<0.001. miR, microRNA; MAG, myelin‑associated <t>glycoprotein;</t> MBP, myelin basic protein; GAP‑43, growth‑associated protein 43; NC, negative control.
    Myelin Associated Glycoprotein, supplied by Bioss, used in various techniques. Bioz Stars score: 90/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/myelin associated glycoprotein/product/Bioss
    Average 90 stars, based on 3 article reviews
    myelin associated glycoprotein - by Bioz Stars, 2026-02
    90/100 stars

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    1) Product Images from "MicroRNA-210 contributes to peripheral nerve regeneration through promoting the proliferation and migration of Schwann cells."

    Article Title: MicroRNA-210 contributes to peripheral nerve regeneration through promoting the proliferation and migration of Schwann cells.

    Journal: Experimental and therapeutic medicine

    doi: 10.3892/etm.2017.4869

    Figure 4. miR‑210 has an effect on the protein levels of GAP‑43, MAG and MBP. (A and B) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of GAP‑43 were detected by western blot analysis. Relative protein levels were calculated using β‑actin as an internal reference. (C and D) The protein levels of MBP were detected by western blot after transfection with miR‑210 mimics or miR‑210 inhibitor. β‑actin was used as an internal reference. (E and F) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of MAG were detected by western blot using β‑actin as an internal reference. All experiments were repeated three times and values are expressed as the mean ± standard deviation. **P<0.01, ***P<0.001. miR, microRNA; MAG, myelin‑associated glycoprotein; MBP, myelin basic protein; GAP‑43, growth‑associated protein 43; NC, negative control.
    Figure Legend Snippet: Figure 4. miR‑210 has an effect on the protein levels of GAP‑43, MAG and MBP. (A and B) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of GAP‑43 were detected by western blot analysis. Relative protein levels were calculated using β‑actin as an internal reference. (C and D) The protein levels of MBP were detected by western blot after transfection with miR‑210 mimics or miR‑210 inhibitor. β‑actin was used as an internal reference. (E and F) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of MAG were detected by western blot using β‑actin as an internal reference. All experiments were repeated three times and values are expressed as the mean ± standard deviation. **P<0.01, ***P<0.001. miR, microRNA; MAG, myelin‑associated glycoprotein; MBP, myelin basic protein; GAP‑43, growth‑associated protein 43; NC, negative control.

    Techniques Used: Transfection, Western Blot, Standard Deviation, Negative Control



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    myelin associated glycoprotein  (Bioss)
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    Bioss myelin associated glycoprotein
    Figure 4. miR‑210 has an effect on the protein levels of GAP‑43, MAG and MBP. (A and B) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of GAP‑43 were detected by western blot analysis. Relative protein levels were calculated using β‑actin as an internal reference. (C and D) The protein levels of MBP were detected by western blot after transfection with miR‑210 mimics or miR‑210 inhibitor. β‑actin was used as an internal reference. (E and F) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of MAG were detected by western blot using β‑actin as an internal reference. All experiments were repeated three times and values are expressed as the mean ± standard deviation. **P<0.01, ***P<0.001. miR, microRNA; MAG, myelin‑associated <t>glycoprotein;</t> MBP, myelin basic protein; GAP‑43, growth‑associated protein 43; NC, negative control.
    Myelin Associated Glycoprotein, supplied by Bioss, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 90 stars, based on 1 article reviews
    myelin associated glycoprotein - by Bioz Stars, 2026-02
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    Figure 4. miR‑210 has an effect on the protein levels of GAP‑43, MAG and MBP. (A and B) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of GAP‑43 were detected by western blot analysis. Relative protein levels were calculated using β‑actin as an internal reference. (C and D) The protein levels of MBP were detected by western blot after transfection with miR‑210 mimics or miR‑210 inhibitor. β‑actin was used as an internal reference. (E and F) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of MAG were detected by western blot using β‑actin as an internal reference. All experiments were repeated three times and values are expressed as the mean ± standard deviation. **P<0.01, ***P<0.001. miR, microRNA; MAG, myelin‑associated <t>glycoprotein;</t> MBP, myelin basic protein; GAP‑43, growth‑associated protein 43; NC, negative control.
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    anti mag antibody  (Bioss)
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    Figure 4. miR‑210 has an effect on the protein levels of GAP‑43, MAG and MBP. (A and B) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of GAP‑43 were detected by western blot analysis. Relative protein levels were calculated using β‑actin as an internal reference. (C and D) The protein levels of MBP were detected by western blot after transfection with miR‑210 mimics or miR‑210 inhibitor. β‑actin was used as an internal reference. (E and F) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of MAG were detected by western blot using β‑actin as an internal reference. All experiments were repeated three times and values are expressed as the mean ± standard deviation. **P<0.01, ***P<0.001. miR, microRNA; MAG, myelin‑associated <t>glycoprotein;</t> MBP, myelin basic protein; GAP‑43, growth‑associated protein 43; NC, negative control.
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    rabbit anti mag antibody  (Bioss)
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    Expression levels of myelin associated inhibitors <t>Nogo-A,</t> <t>OMgp</t> and <t>MAG</t> in ischemic rat brains. Immunohistochemical staining of (A) Nogo-A, (B) OMgp and (C) MAG, in middle cerebral artery occlusion and MSCs groups at day 14 after MCAO (magnification, ×200; n=10 per group). OMgp, Oligodendrocyte myelin glycoprotein; MAG, myelin-associated glycoprotein; PBS, phosphate-buffered saline MSCs, mesenchymal stem cells.
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    Image Search Results


    Figure 4. miR‑210 has an effect on the protein levels of GAP‑43, MAG and MBP. (A and B) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of GAP‑43 were detected by western blot analysis. Relative protein levels were calculated using β‑actin as an internal reference. (C and D) The protein levels of MBP were detected by western blot after transfection with miR‑210 mimics or miR‑210 inhibitor. β‑actin was used as an internal reference. (E and F) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of MAG were detected by western blot using β‑actin as an internal reference. All experiments were repeated three times and values are expressed as the mean ± standard deviation. **P<0.01, ***P<0.001. miR, microRNA; MAG, myelin‑associated glycoprotein; MBP, myelin basic protein; GAP‑43, growth‑associated protein 43; NC, negative control.

    Journal: Experimental and therapeutic medicine

    Article Title: MicroRNA-210 contributes to peripheral nerve regeneration through promoting the proliferation and migration of Schwann cells.

    doi: 10.3892/etm.2017.4869

    Figure Lengend Snippet: Figure 4. miR‑210 has an effect on the protein levels of GAP‑43, MAG and MBP. (A and B) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of GAP‑43 were detected by western blot analysis. Relative protein levels were calculated using β‑actin as an internal reference. (C and D) The protein levels of MBP were detected by western blot after transfection with miR‑210 mimics or miR‑210 inhibitor. β‑actin was used as an internal reference. (E and F) After transfection with miR‑210 mimics or miR‑210 inhibitor, the protein levels of MAG were detected by western blot using β‑actin as an internal reference. All experiments were repeated three times and values are expressed as the mean ± standard deviation. **P<0.01, ***P<0.001. miR, microRNA; MAG, myelin‑associated glycoprotein; MBP, myelin basic protein; GAP‑43, growth‑associated protein 43; NC, negative control.

    Article Snippet: The membranes were blocked with 5% skimmed milk, followed by incubation with primary antibodies against growth-associated protein-43 (GAP-43; 1:200 dilution; Santa Cruz Biotechnologies, Inc., Dallas, TX, USA; cat. no. sc-33705), myelin-associated glycoprotein (MAG; 1:500 dilution; Bioss, Beijing, China; cat no. bs-0257R), myelin basic protein (MBP; 1:500 dilution; Bioss; cat. no. bs-0380R) and β‐actin (1:1,000, Santa Cruz Biotechnologies, Inc.) at 4 ̊C overnight.

    Techniques: Transfection, Western Blot, Standard Deviation, Negative Control

    Expression levels of myelin associated inhibitors Nogo-A, OMgp and MAG in ischemic rat brains. Immunohistochemical staining of (A) Nogo-A, (B) OMgp and (C) MAG, in middle cerebral artery occlusion and MSCs groups at day 14 after MCAO (magnification, ×200; n=10 per group). OMgp, Oligodendrocyte myelin glycoprotein; MAG, myelin-associated glycoprotein; PBS, phosphate-buffered saline MSCs, mesenchymal stem cells.

    Journal: Experimental and Therapeutic Medicine

    Article Title: Transplantation of mesenchymal stem cells promotes the functional recovery of the central nervous system following cerebral ischemia by inhibiting myelin-associated inhibitor expression and neural apoptosis

    doi: 10.3892/etm.2016.3089

    Figure Lengend Snippet: Expression levels of myelin associated inhibitors Nogo-A, OMgp and MAG in ischemic rat brains. Immunohistochemical staining of (A) Nogo-A, (B) OMgp and (C) MAG, in middle cerebral artery occlusion and MSCs groups at day 14 after MCAO (magnification, ×200; n=10 per group). OMgp, Oligodendrocyte myelin glycoprotein; MAG, myelin-associated glycoprotein; PBS, phosphate-buffered saline MSCs, mesenchymal stem cells.

    Article Snippet: The primary antibodies used in the study were as follows: Rabbit anti-Caspase-3 polyclonal antibody (1:100; PA5-16335; LabVision/Neomarkers; Thermo Fisher Scientific, Inc.), rabbit anti-Bcl-2 antibody (1:80; sc-492; Santa Cruz Biotechnology, Inc., Dallas, TX, USA), rabbit anti-Nogo-A antibody (1:30; PA1060; Wuhan Boster Biological Technology, Ltd., Wuhan, China), rabbit anti-OMgp antibody (1:80; BS-1200R; BIOSS, Beijing, China) and rabbit anti-MAG antibody (1:100; BS-0257R; BIOSS).

    Techniques: Expressing, Immunohistochemical staining, Staining